In this part of his Pharmaceutical Executive video interview, Ian Chan, CEO of Abpro gives an update on the preclinical development of Abpro's lead HER2/CD3 T cell engager.
Ian Chan, CEO of Abpro, discusses the advantages of their DiversImmune and MultiMab platforms for antibody discovery and engineering. Abpro's platform can create novel antibodies at industry-leading speeds, which are then reassembled into custom configurations for therapeutic purposes. They have developed bispecific antibodies, particularly T cell engagers for oncology, which are effective against solid tumors. Abpro's lead oncology program for breast cancer, in partnership with Celltrion, is advancing through clinical phases. Additionally, they have an eye care molecule targeting AMD and DME. The recent NASDAQ listing will aid in accelerating R&D and commercialization efforts. Collaborations, like the one with Celltrion, have been instrumental in the company's success.
The team's been working for a number of years on this, so I think there, this is where our platform was very helpful. We were able to cycle. Through different generations and types of antibodies that we felt would be ultimately the optimal solution for her two was a hard target, so we were able to iterate very quickly early on in the development cycle. So that was step one, and then being able to test them very rapidly was also very important. So as different configurations came out, being able to test them in vitro and also in vivo, to quickly see that there was high safety and also tumor killing. So that happened fairly early on in the life cycle, in certain building blocks had to be created, I would say, on a custom basis, um, in house, for example, proprietary CD3 arm that would allow us to progress through the clinic hopefully much faster. We built that in there were custom building blocks, a lot of iterations that were performed very quickly to get to the final configuration. And then, and then the in vivo work is, I would say, you know, people call it more development type work as we progress toward the clinic. We've done all that as well. And then the factoring, because the molecule was designed to be easily manufacturable, has been straightforward so far so, so that's been the evolution of this molecule.
Key Findings of the NIAGARA and HIMALAYA Trials
November 8th 2024In this episode of the Pharmaceutical Executive podcast, Shubh Goel, head of immuno-oncology, gastrointestinal tumors, US oncology business unit, AstraZeneca, discusses the findings of the NIAGARA trial in bladder cancer and the significance of the five-year overall survival data from the HIMALAYA trial, particularly the long-term efficacy of the STRIDE regimen for unresectable liver cancer.
Cell and Gene Therapy Check-in 2024
January 18th 2024Fran Gregory, VP of Emerging Therapies, Cardinal Health discusses her career, how both CAR-T therapies and personalization have been gaining momentum and what kind of progress we expect to see from them, some of the biggest hurdles facing their section of the industry, the importance of patient advocacy and so much more.